HeLa Cells: Why Most People Get the Story Wrong

HeLa Cells: Why Most People Get the Story Wrong

You’ve probably heard of them in a biology class or maybe while scrolling through a bookstore and seeing that famous yellow cover of Rebecca Skloot’s book. HeLa cells are everywhere. Literally. They are in labs in London, refrigerators in Tokyo, and probably in the vaccine vial you got at the pharmacy last year. They are the first "immortal" human cell line, meaning they don't just die off after a few divisions like normal cells do. They just keep going.

It’s wild.

But here is the thing: for decades, most of the scientific community didn't even know where they came from. They were just a tool. A biological "workhorse." Most people didn't know the name Henrietta Lacks. They didn't know about the young Black mother of five who walked into Johns Hopkins Hospital in 1951 with a "knot" in her womb. They didn't know that while she was being treated for a particularly aggressive form of cervical cancer, a surgeon took a snippet of her tumor without asking her or telling her.

She died shortly after. Her cells, however, never did.

What Are HeLa Cells and Why Do They Keep Growing?

Usually, when you put human cells in a petri dish, they poop out. It’s called the Hayflick Limit. Basically, normal cells can only divide about 40 to 60 times before they hit a programmed death. It’s a safety mechanism. But HeLa cells are different. They are aggressive. Because they came from a malignant adenocarcinoma, they had already bypassed the body's natural "stop" signals.

They have an overactive version of an enzyme called telomerase.

Think of telomeres like the plastic tips on shoelaces. Every time a cell divides, those tips get shorter. When they're gone, the cell dies. In HeLa cells, the telomerase keeps rebuilding those tips. They never get shorter. They are, for all intents and purposes, biologically immortal. This wasn't just a lucky break for science; it was a revolution. Before 1951, researchers spent more time trying to keep cells alive than actually studying them. Suddenly, George Gey, the researcher at Hopkins who first cultured them, had a factory that produced new cells every 24 hours.

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He started mailing them to scientists in padded envelopes. Just like that, the world of medicine changed forever.

The Scientific Impact You Benefit From Today

It is almost impossible to overstate how much of modern medicine relies on these cells. If you’ve ever had a vaccine, used a certain type of makeup, or taken a prescription drug, you've likely benefited from Henrietta's cells.

  • The Polio Vaccine: In the 1950s, Jonas Salk needed a massive amount of human cells to test his polio vaccine. HeLa was the answer. They were the first cells to be mass-produced in a factory setting.
  • Gene Mapping: Scientists used them to help map the human genome.
  • COVID-19: More recently, researchers used HeLa to understand how the SARS-CoV-2 virus enters human cells.
  • Cancer Research: Because they are cancer cells, they’ve been used to study how tumors grow and how to kill them with chemotherapy or radiation without destroying the rest of the body.

The list goes on. They’ve been sent into space to see how zero gravity affects human tissue. They’ve been used to study the effects of the atomic bomb. Honestly, if there’s a major medical breakthrough in the last 70 years, HeLa probably had a hand in it.

The Ethical Mess That Science Ignored

For a long time, the narrative was focused solely on the "miracle" of the cells. But there is a dark side to this. Henrietta Lacks was a Black woman in the Jim Crow era receiving care in a segregated ward. The doctors at Johns Hopkins didn't get her consent to take the tissue for research. Back then, "informed consent" wasn't really a thing in the way it is today, but the racial dynamics cannot be ignored.

While companies made billions of dollars selling HeLa-related products and technologies, the Lacks family lived in poverty.

They didn't even find out the cells existed until the 1970s. Imagine finding out through a random phone call or a news snippet that parts of your mother are living in thousands of labs across the globe. It was a massive violation of privacy. The family's medical records were published without permission. Their own DNA was sequenced and put online without a "hey, is this okay?"

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It wasn't until much later—specifically after the massive success of the 2010 book The Immortal Life of Henrietta Lacks—that the conversation shifted toward justice.

Recent Settlements and the Path Forward

In 2023, there was a major breakthrough. The Lacks family settled a lawsuit against Thermo Fisher Scientific. The lawsuit argued that the company had unjustly enriched itself by mass-producing and selling the cells without the family's permission. It was a landmark moment. It wasn't just about the money; it was about the acknowledgement. It was the first time a major corporation was held accountable for using these specific "stolen" materials.

But it’s complicated. If you stop using HeLa cells today, global research stalls. You can't just "undo" 70 years of science. What we can do is change how we handle biospecimens going forward.

Dealing With "HeLa Contamination"

Here is a weird fact that most people don't know: HeLa cells are so aggressive that they actually ruin other experiments.

They are like the kudzu of the lab world. Because they grow so fast and travel so easily—on dust particles, on unwashed gloves, in the air—they often "infect" other cell cultures. For decades, scientists thought they were studying breast cancer or prostate cancer, only to find out years later that HeLa cells had crawled into the dish and taken over.

Some researchers estimate that up to 20% of all cell line research might be tainted by HeLa contamination. It’s a legitimate crisis in the scientific community called "cell line misidentification." It has led to retracted papers and millions of dollars in wasted grant money. It turns out that Henrietta’s cells are so powerful they can essentially "out-compete" almost any other cell they come into contact with.

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Why This Matters to You

You might think this is all high-level lab stuff, but it hits home. It forces us to ask: Who owns your body once you leave the doctor's office?

Currently, in many places, once a piece of you (a mole, an appendix, a blood sample) is removed, it is often considered "medical waste." Researchers can often use that waste for study without specifically telling you exactly what they are doing with it, provided it is "de-identified." The HeLa story is the reason we have the "Common Rule" in the U.S., which sets ethical standards for human subject research.

It’s about dignity. It’s about the fact that Henrietta Lacks was a person, not just a catalog number in a lab.

Actionable Steps for the Informed Patient

If you want to be proactive about your own biological data and tissue, there are a few things you can actually do. Science needs samples to cure diseases, but you have the right to know how yours are being used.

  1. Read the Fine Print: When you sign those stacks of papers at a hospital before a procedure, look for the "Research Consent" section. You can often opt-out of having your "discarded" tissue used for future research.
  2. Ask About Biobanks: If you are participating in a study, ask if your samples will be stored in a biobank and who will have access to them.
  3. Support Ethical Science: Organizations like the Henrietta Lacks Foundation provide grants to the Lacks family and others who have been used in research without consent. Supporting these initiatives helps bridge the gap between scientific progress and restorative justice.
  4. Check Your Source: If you are a student or researcher, always verify your cell lines. Use tools like the International Cell Line Authentication Committee (ICLAC) database to ensure you aren't accidentally working with a contaminated HeLa strain.

The legacy of HeLa cells is a double-edged sword. It is a story of incredible life-saving triumph and a story of systemic exploitation. We have the polio vaccine because of Henrietta Lacks. We have treatments for HPV because of her. But we also have a massive ethical debt that the scientific community is only just beginning to pay back. Henrietta’s cells changed the world, but it’s our job to make sure the world remembers the woman behind the microscope.